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The mutation is a C-to-T transition at nucleotide position 275 (Genbank Accession NM_031397) resulting in replacement of threonine by isoleucine at amino acid position 86 (T86I), which resides in the N-terminal K homology RNA-binding domain of the protein. (J:132744)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
